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Displaying 20 of 379 results for "MECP2"
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  1. Macaca mulatta : TALEN-mediated MeCP2 Gene Mutagenesis in Rhesus and Cynomolgus Monkeys BioProject

    ID: PRJNA230664

    Keywords: transcriptome

    Access Type: download

  2. MeCP2 binds to mCH as neurons mature, influencing transcription and onset of Rett syndrome [ChIP-Seq] BioProject

    ID: PRJNA278146

    Keywords: Epigenomics

    Access Type: download

  3. Transcriptional regulation in pluripotent stem cells by Methyl CpG binding protein 2 (MeCP2) BioProject

    ID: PRJNA224073

    Keywords: Transcriptome or Gene expression

    Access Type: download

  4. Cerebellar gene expression data from Mecp2-null and MECP2-transgenic mice BioProject

    ID: PRJNA115751

    Keywords: Transcriptome or Gene expression

    Access Type: download

  5. Mus musculus : Mus musculus Transcriptome or Gene expression BioProject

    ID: PRJNA226996

    Keywords: transcriptome

    Access Type: download

    dataset.description: Mutations in MeCP2 causes the neurological disorder Rett syndrome. We compare gene expression changes in t...
  6. Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function BioProject

    ID: PRJNA112167

    Keywords: Transcriptome or Gene expression

    Access Type: download

  7. uman super frontal gyrus (post mortem brain) from Rett syndrome patients and age sex matched controls reveals FXYD1, an MeCP2 target gene overexpressed in the brains of ArrayExpress

    ID: E-GEOD-6955

    Description: Rett syndrome (RTT, OMIM 312750) is a severe X-linked neurodevelopmental disorder linked to heterozygous de novo...

  8. Hypothalamic gene expression data from Mecp2-null and MECP2-transgenic mice BioProject

    ID: PRJNA106951

    Keywords: Transcriptome or Gene expression

    Access Type: download

  9. Astrocyte transcriptome from Mecp2-deficient mice BioProject

    ID: PRJNA244332

    Keywords: Transcriptome or Gene expression

    Access Type: download

  10. MeCP2 binds to mCH as neurons mature, influencing transcription and onset of Rett syndrome [mRNA-Seq] BioProject

    ID: PRJNA278144

    Keywords: Transcriptome or Gene expression

    Access Type: download

  11. Cerebellar gene expression data from Mecp2-null and MECP2-transgenic mice ArrayExpress

    ID: E-GEOD-15574

    Description: ression changes in the cerebellum of mice lacking MeCP2 (Mecp2-null) and mice overexpressing MeCP2 (MECP2-transgenic). A group of postnatal neu...

  12. MeCP2 binds to mCH as neurons mature, influencing transcription and onset of Rett syndrome [Mnase-Seq] BioProject

    ID: PRJNA278145

    Keywords: Epigenomics

    Access Type: download

  13. Hypothalamic gene expression data from Mecp2-null and MECP2-transgenic mice ArrayExpress

    ID: E-GEOD-11150

    Description: ssion changes in the hypothalamus of mice lacking MeCP2 (Mecp2-null) and mice overexpressing MeCP2 (MECP2-transgenic). Mutations in the gene encod...

  14. Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function ArrayExpress

    ID: E-GEOD-14715

    Description: Mutations of MECP2 (Methyl-CpG Binding Protein 2)...

  15. Mecp2: an unexpected regulator of macrophage gene expression and function [ChIP-Seq] BioProject

    ID: PRJNA277172

    Keywords: Epigenomics

    Access Type: download

  16. Transcriptional regulation in pluripotent stem cells by Methyl CpG binding protein 2 (MeCP2) ArrayExpress

    ID: E-GEOD-51607

    Description: Rett syndrome (RTT) is one of the most prevalent female mental disorders. De novo mutations in methyl

  17. MeCP2 binds to mCH as neurons mature, influencing transcription and onset of Rett syndrome [mRNA-Seq] ArrayExpress

    ID: E-GEOD-66870

    Description: The postnatal neurodevelopmental disorder Rett syndrome (RTT) is caused by mutations in the gene encoding Methyl-CpG...

  18. Mus musculus : Mus musculus Genome sequencing BioProject

    ID: PRJNA230805

    Keywords: genome sequencing

    Access Type: download

    dataset.description: Mutations in MeCP2 causes the neurological disorder Rett syndrome. We use chromatin immunoprecipitation of...
  19. MeCP2 binds to mCH as neurons mature, influencing transcription and onset of Rett syndrome [ChIP-Seq] ArrayExpress

    ID: E-GEOD-66868

    Description: The postnatal neurodevelopmental disorder Rett syndrome (RTT) is caused by mutations in the gene encoding Methyl-CpG...

  20. MeCP2 binds to mCH as neurons mature, influencing transcription and onset of Rett syndrome [Mnase-Seq] ArrayExpress

    ID: E-GEOD-66869

    Description: The postnatal neurodevelopmental disorder Rett syndrome (RTT) is caused by mutations in the gene encoding Methyl-CpG...


Displaying 20 of 379 results for "MECP2"